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Applied and Environmental Microbiology, December 2000, p. 5426-5436, Vol. 66, No. 12
0099-2240/00/$04.00+0
Detection on Surfaces and in Caco-2 Cells of Campylobacter
jejuni Cells Transformed with New gfp, yfp, and
cfp Marker Plasmids
William G.
Miller,*
Anne H.
Bates,
Sharon T.
Horn,
Maria T.
Brandl,
Marian R.
Wachtel, and
Robert E.
Mandrell
Food Safety and Health Research Unit, Agricultural
Research Service, U.S. Department of Agriculture, Albany,
California 94710
Received 1 June 2000/Accepted 16 August 2000
We have developed two sets of Campylobacter shuttle
vectors containing either the gfp (green fluorescent
protein), yfp (yellow fluorescent protein), or
cfp (cyan fluorescent protein) reporter gene. In one set,
the reporter gene is fused to a consensus Campylobacter promoter sequence (Pc). The other set contains a pUC18
multicloning site upstream of the reporter gene, allowing the
construction of transcriptional fusions using known promoters or random
genomic fragments. C. jejuni cells transformed with the
Pc fusion plasmids are strongly fluorescent and easily
visualized on chicken skin, on plant tissue, and within infected Caco-2
cells. In each C. jejuni strain tested, these plasmids were
maintained over several passages in the absence of antibiotic
selection. Also, in many C. jejuni strains, >91% of the
cells transformed with the Pc fusion plasmids remained
fluorescent after several days. Experiments with yellow fluorescent and
cyan fluorescent C. jejuni transformants suggest that
aggregates containing two or more strains of C. jejuni may
be present in an enrichment broth culture. Colonies arising from these
aggregates would be heterologous in nature; therefore, isolation of a
pure culture of C. jejuni, by selecting single colonies,
from an environmental sample may not always yield a single strain.
*
Corresponding author. Mailing address: USDA, ARS, WRRC,
Food Safety and Health Research Unit, 800 Buchanan St., Albany, CA 94710. Phone: (510) 559-5992. Fax (510) 559-6162. E-mail:
bmiller{at}pw.usda.gov.
Applied and Environmental Microbiology, December 2000, p. 5426-5436, Vol. 66, No. 12
0099-2240/00/$04.00+0
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